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Volumn 13, Issue 9, 2011, Pages 2334-2337

An approach to the core structure of leiodermatolide

Author keywords

[No Author keywords available]

Indexed keywords

LEIODERMATOLIDE; MACROLIDE;

EID: 79955595872     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200584a     Document Type: Article
Times cited : (24)

References (48)
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    • Chem. Abstr. 2008, 148, 230104.
    • (2008) Chem. Abstr. , vol.148 , pp. 230104
  • 3
    • 79955616384 scopus 로고    scopus 로고
    • 50 values were reported in the patent: A549, P399 = 3.3 nM, PANC-1 = 5.0 nM, DLD-1 = 8.3 nM, NCI-ADR-Res = 233 nM.
    • 50 values were reported in the patent: A549, P399 = 3.3 nM, PANC-1 = 5.0 nM, DLD-1 = 8.3 nM, NCI-ADR-Res = 233 nM.
  • 4
    • 79955580469 scopus 로고    scopus 로고
    • Accessed on March 25.
    • http://www.rsmas.miami.edu/groups/ohh/courses/ 23nov12wrightmarinenaturalproductsdrugdiscovery.pdf. Accessed on March 25, 2011.
    • (2011)
  • 12
    • 79955587699 scopus 로고    scopus 로고
    • A ring-closing metathesis strategy (formation of the C4-C5 double bond) did not work in our hands. Ph.D. Thesis, University of Tübingen.
    • A ring-closing metathesis strategy (formation of the C4-C5 double bond) did not work in our hands. Vaidotas, N. Ph.D. Thesis, University of Tübingen, 2011.
    • (2011)
    • Vaidotas, N.1
  • 13
    • 79955623081 scopus 로고    scopus 로고
    • Coupling of a C1-C11 vinylstannane with a C12-C18 vinyl iodide (1-OTBS) did not give the corresponding conjugated diene.
    • Coupling of a C1-C11 vinylstannane with a C12-C18 vinyl iodide (1-OTBS) did not give the corresponding conjugated diene.
  • 18
    • 79955629023 scopus 로고    scopus 로고
    • Wiley: New York,; Collect. Vol., pp
    • Organic Synthesis; Wiley: New York, 2009; Collect. Vol. XI, pp 1056-1067
    • (2009) Organic Synthesis , vol.11 , pp. 1056-1067
  • 27
    • 0000830549 scopus 로고
    • Wiley: New York,; Collect. Vol., pp
    • Organic Synthesis; Wiley: New York, 1993; Collect. Vol. VIII, pp 339-343
    • (1993) Organic Synthesis , vol.8 , pp. 339-343
  • 37
    • 79955642006 scopus 로고    scopus 로고
    • Substrate 33 with a TBS protecting group at 1-OH instead of the pivaloyl group did not react in the Stille cross-coupling.
    • Substrate 33 with a TBS protecting group at 1-OH instead of the pivaloyl group did not react in the Stille cross-coupling.
  • 44


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.